15212020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3228476-C-T

15212202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3228297-A-G

15212226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3228273-T-C

http://identifiers.org/hco/10/GRCh38#15212391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3228032-C-A

15212391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3228032-C-T

15212392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3228031-G-A

15212392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3228031-G-T

15212411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3228012-A-T

15212466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3227959-G-A

15212466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3227959-G-T

15212484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3227941-C-G

15212484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3227941-C-T

15212532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3227894-A-G

15212561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3227857-T-G

15212638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3227780-T-A

15212638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3227780-T-C

http://identifiers.org/hco/10/GRCh38#15212673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3227747-C-A

http://identifiers.org/hco/10/GRCh38#15212686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3227742-C-A

15212686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3227742-C-G

15212686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3227742-C-T

15212890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3227570-C-T

http://identifiers.org/hco/10/GRCh38#15212922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3227538-A-C

15212922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3227538-A-G

15213000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3227460-T-C

15213147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3227307-C-T

15213162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3227292-T-A

http://identifiers.org/hco/10/GRCh38#15213175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3227279-C-A

15213175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3227279-C-G

15213297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3227157-T-G

15213369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3227085-A-G

15213519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3226935-T-A

15213636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3226818-G-A

15213636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3226818-G-C

15213636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3226818-G-T

15213698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 3226756-G-C

15213801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3226653-T-C

15214044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3226410-A-G

15214067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 3226387-G-C

15214110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3226344-A-G

15214172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3226282-C-T

15214356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3226098-T-A

15214356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3226098-T-G

http://identifiers.org/hco/10/GRCh38#15214376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3226078-C-A

15214376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 3226078-C-G

15214376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 3226078-C-T

http://identifiers.org/hco/10/GRCh38#15214730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3225743-C-A

15214752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3225718-C-T

15215715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3225527-G-C

15215751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3225494-T-C

http://identifiers.org/hco/10/GRCh38#15215834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3224777-C-A

15216217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3224384-A-G

15216227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3224373-G-T

15217279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3223628-G-A

15218890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3222739-C-T

15218992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3222619-G-C

15219968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3222320-C-T

15219974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3222314-T-C

http://identifiers.org/hco/10/GRCh38#15220078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3222203-A-C

15220223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3222059-G-T

15220226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3222056-T-C

15220367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3221951-C-G

15220517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3221808-G-C

15220906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3221442-A-G

15220907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3221441-C-G

15221367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3221009-C-T

15221382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3220991-G-A

15221382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3220991-G-T

15221714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3220658-A-G

15222141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3220201-G-A

15222141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3220201-G-T

15222193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3220148-C-G

15222853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3219862-C-T

http://identifiers.org/hco/10/GRCh38#15223370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3219487-A-C

15223505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3219362-C-T

http://identifiers.org/hco/10/GRCh38#15224092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3219147-A-C

15224200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3219075-C-T

15224246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3219042-T-A

15224246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3219042-T-C

15225034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3218622-G-A

15225034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3218622-G-T

15225327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3217918-A-G

15225349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3217897-G-C

15225759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3217393-G-C

http://identifiers.org/hco/10/GRCh38#15225792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3217290-C-A

15225792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3217290-C-T

15225944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3217004-A-G

15225992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3216959-T-A

15226060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3216867-C-T

15226500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3216474-G-A

15227830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3215415-G-A

15227830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3215415-G-T

15227864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3215381-T-C

15228158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3215130-T-A

15228179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3215109-C-G

15228179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3215109-C-T

http://identifiers.org/hco/10/GRCh38#15228809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3214848-C-A

15228809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3214848-C-T

15228827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3214830-G-A

15228855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3214805-C-T

15229001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3214682-T-C

15230561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3214266-C-T

15234171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3212686-T-A

15234171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3212686-T-G

http://identifiers.org/hco/10/GRCh38#15234193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3212664-C-A

15235906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3211671-G-C

15236272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3211328-T-A

15236324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3211288-A-G

15237181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3210116-T-C

15237317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3209925-C-T

15237372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3209884-T-A

15237384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3209871-G-A

15237384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3209871-G-T

15237664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 3209608-G-A

15237664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 3209608-G-T

15237778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3209540-C-T

15238025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3209193-T-C

15238062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3209156-T-C

15238160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3209058-T-A

15238160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3209058-T-C

15238204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3209016-G-C

15238463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3208795-T-C

15238592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3208664-C-T

http://identifiers.org/hco/10/GRCh38#15238725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3208533-C-A

15238778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3208480-C-G

15238862-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3208396-T-A

15239033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3208228-T-C

http://identifiers.org/hco/10/GRCh38#15239265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3208031-C-A

15241658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3206456-C-G

15241744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3206373-G-T

15241995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3206116-C-T

15242013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3206099-C-T

15247826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3204351-A-G

15247837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3204340-A-G

15247938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3204239-T-C

15248049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3204130-T-G

15248058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3204121-G-A

http://identifiers.org/hco/10/GRCh38#15248661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3203734-C-A

15248661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3203734-C-G

15248661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3203734-C-T

15248725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: missense variant
orthologous variants: 3203670-G-A

http://identifiers.org/hco/10/GRCh38#15248840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3203556-C-A

15248840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3203556-C-T

http://identifiers.org/hco/10/GRCh38#15248846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3203550-C-A

15248846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3203550-C-T

15249674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3202474-G-A

15249839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3202311-T-C

http://identifiers.org/hco/10/GRCh38#15249921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3202230-C-A

15250099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3201958-T-C

15250414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3201668-C-T

15251743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3200822-A-T

15251747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3200818-T-G

15251803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3200759-A-G

15251811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3200751-T-G

http://identifiers.org/hco/10/GRCh38#15251824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3200738-C-A

15251824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3200738-C-T

15251985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3200605-A-T

15252510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3200222-G-A

http://identifiers.org/hco/10/GRCh38#15252549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3200185-C-A

15252594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3200142-C-T

15252715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3200018-C-T

15253540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3199585-C-T

15253590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3199541-T-C

15253622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3199510-C-T

15253681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3199451-C-G

15253682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3199450-T-C

15253803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3199349-T-C

15253963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3199238-T-C

15254143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3199029-G-C

http://identifiers.org/hco/10/GRCh38#15254155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3199017-C-A

15254159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3199013-G-C

http://identifiers.org/hco/10/GRCh38#15254300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3198874-C-A

15254437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3198751-A-G

15254587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3198606-T-A

15254587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3198606-T-C

http://identifiers.org/hco/10/GRCh38#15254614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3198579-A-C

15254614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3198579-A-G

15254614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3198579-A-T

15254620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3198570-T-C

15254656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3198533-T-C

15254759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant
orthologous variants: 3198432-C-G

15254807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, missense_variant
orthologous variants: 3198384-T-C

15254963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3198248-G-T

http://identifiers.org/hco/10/GRCh38#15254981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3198230-C-A

15254981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3198230-C-T

http://identifiers.org/hco/10/GRCh38#15254985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3198224-C-A

15254985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3198224-C-T

http://identifiers.org/hco/10/GRCh38#15255029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3198180-C-A

15255145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3198064-T-A

15255165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3198042-C-T

15255430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3197776-C-T

15255474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3197735-G-A

15256014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3197543-C-T

15256399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3197149-A-G

15256817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3196823-T-C

15257220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3196498-C-T

15257473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3196318-C-G

15257473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3196318-C-T

15257639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3196108-A-G

15257652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3196095-G-A

15257863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3195874-C-T

15258302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3195682-C-T

15258619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3195394-C-T

http://identifiers.org/hco/10/GRCh38#15258659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3195360-C-A

15258659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3195360-C-T

15258663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3195357-A-G

15258690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3195327-T-A

15258735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3195284-G-T

15258900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3195132-C-T

15258907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3195127-T-C

15259014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3195037-T-C

15259080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3194986-G-A

15259255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3194861-A-G

15259424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3194711-C-T

15260705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3194007-C-G

15260781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3193944-T-A

15260781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3193944-T-C

15260881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3193841-G-A

15260881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3193841-G-C

15260896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3193826-C-T

15261020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3193695-C-T

15261624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3193572-T-A

15261735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3193469-C-T

15261763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3193441-G-A

15262343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3193278-G-A

15262789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3192819-G-A

15262980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3192655-C-G

15262980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3192655-C-T

15264996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3190974-C-T

15265106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3190859-A-T

15265588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3190727-A-G

15265594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3190721-A-G

15265625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3190691-A-T

15265630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3190686-G-A

15265630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3190686-G-T

15265756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3190579-T-A

15269451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3188081-A-G

15269498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3188031-T-G

15269812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3187724-T-C

15269812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3187724-T-G

15269858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3187673-T-C

15269896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3187636-C-T

http://identifiers.org/hco/10/GRCh38#15276006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3187398-C-A

15276006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3187398-C-G

15276006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3187398-C-T

15276065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3187343-T-A

15276129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3187297-T-C

15276367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3187019-T-C

15276512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3186934-C-T

15276541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3186905-T-C

15278961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3183402-G-T

15279019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3183367-C-T

15279187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3182763-T-A

15279571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3182314-A-G

15279616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3182273-T-C

15280211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3182175-G-T

15280448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3181580-G-A

15280478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3181550-T-C

15280539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3181493-G-A

15280632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3181414-A-T

15280755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3181305-C-G

15280883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3181181-T-C

15280916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3181149-G-A

15283922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: missense variant
orthologous variants: 3179454-G-C

15284969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3178150-G-A

http://identifiers.org/hco/10/GRCh38#15284997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3178122-C-A

http://identifiers.org/hco/10/GRCh38#15285128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3177994-A-C

15285173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3177946-C-T

http://identifiers.org/hco/10/GRCh38#15285333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3177810-C-A

15285333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3177810-C-T

15288522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3176095-G-A

15288587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3176030-T-G

15288775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3175868-G-A

15294098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3174478-G-A

15294345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3174182-G-T

15294424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3174039-T-A

15294428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3174035-T-C

15294504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3173958-C-G

15294621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3173843-G-A

15294621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3173843-G-C

15294735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3173726-G-A

15294735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3173726-G-C

15294735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3173726-G-T

15294776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3173685-A-G

15294799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3173648-G-T

http://identifiers.org/hco/10/GRCh38#15294818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3173629-A-C

15295431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3173336-A-T

15295885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3172910-G-A

15295885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3172910-G-C

15297511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3171482-T-C

15297619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3171380-T-C

15297663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3171291-A-G

15297794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3171116-T-G

15297993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3170933-A-G

15298749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3170582-C-G

15298749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3170582-C-T

http://identifiers.org/hco/10/GRCh38#15298812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3170523-C-A

15299410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3170278-G-C

15299410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3170278-G-T

15299422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3170266-C-T

15299456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3170237-T-A

15299632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3170088-A-G

15300058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3169956-T-C

15300487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3169456-A-G

http://identifiers.org/hco/10/GRCh38#15300630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3169215-A-C

15301670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3168532-C-T

http://identifiers.org/hco/10/GRCh38#15301715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3168489-C-A

15301727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3168477-C-T

15301809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3168421-C-G

15301818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3168412-C-T

15301896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3168342-G-C

15301909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3168329-T-C

15301945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3168302-G-A

15302122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3168151-A-G

15302174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3168097-T-A

15302174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3168097-T-C

http://identifiers.org/hco/10/GRCh38#15303307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3167679-C-A

15303369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3167598-C-T

15303612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3167402-A-T

15303819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3166337-G-A

15303866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3166290-G-A

15304179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3166020-G-C

15304404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3165805-C-T

15304475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3165737-G-A

http://identifiers.org/hco/10/GRCh38#15304549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3165674-C-A

15304797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3165504-C-T

15304861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3165476-C-T

15305122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3165307-A-T

15310042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3163413-A-G

15310061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3163394-C-T

15310077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3163378-T-A

15310167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3163309-C-T

15310224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3163266-T-A

15311086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3162735-T-C

15311086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3162735-T-G

15311504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3162317-A-G

15313055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3160723-G-C

15313137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3160642-T-C

15313428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3160304-T-C

15313428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3160304-T-G

15313446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3160286-T-C

15313488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3160244-G-A

15313491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3160241-A-G

15313522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3160215-G-A

15313817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3159921-G-C

15313817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3159921-G-T

15313857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3159885-C-T

15313878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3159862-T-A

15314097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3159649-T-C

http://identifiers.org/hco/10/GRCh38#15314118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3159626-C-A

15314118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3159626-C-T

15320878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3157375-T-G

15320908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3157346-G-C

15320908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3157346-G-T

15321075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3157199-T-G

15321821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, undefined
orthologous variants: 3156653-G-A

15321871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3156603-A-T

15321894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3156580-C-T

15322199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3156285-A-G

15322503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3156004-T-C

15322725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3155819-T-C

15322767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3155794-A-G

15323872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3155332-T-A

15324362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3154917-T-C

15324564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3154751-C-T

15324940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3154464-A-G

15325904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, undefined
orthologous variants: 3151707-G-C

15325904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, undefined
orthologous variants: 3151707-G-T

15326217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3151377-C-T

15328861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3149889-G-A

15328918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3149832-C-T

http://identifiers.org/hco/10/GRCh38#15328933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3149817-A-C

http://identifiers.org/hco/10/GRCh38#15329382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3149374-C-A

15329382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3149374-C-T

15329652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3149213-G-T

15329658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3149208-T-A

15329665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3149195-G-A

15334143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3146832-T-G

15334498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 3146593-T-C

15334742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 3146393-G-A

15335538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3144811-G-A

15335538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3144811-G-C

15335734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3144644-A-G

15335803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3144541-A-G

15335882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3144390-T-C

15336017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3144255-A-T

http://identifiers.org/hco/10/GRCh38#15336201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3143721-A-C

15336318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3143606-T-C

15345077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, undefined
orthologous variants: 3140753-T-C

15345121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3140701-C-T

15349630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3136492-G-A

15349630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3136492-G-T

15350358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3135874-G-A

15350531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3135685-C-T

15350607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3135622-C-T

15351117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3135303-C-T

15351357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3135073-G-A

15351404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3135025-A-G

http://identifiers.org/hco/10/GRCh38#15352435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3134516-C-A

15352468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3134485-T-C

15352710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3134255-A-G

15352726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3134238-C-G

15352757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3134209-T-C

http://identifiers.org/hco/10/GRCh38#15352922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3133927-A-C

15353099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3133738-T-C

15353528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3130131-T-C

15358441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3126121-T-C

15358573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3125991-A-G

15358608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3125972-T-G

15358720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3125878-C-T

http://identifiers.org/hco/10/GRCh38#15358883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3125713-C-A

15358883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3125713-C-T

15361126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3123990-T-C

15368655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3121891-A-T

15369342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3121205-C-T

15369506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3121050-G-A

15369743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3120837-C-T

15370175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3120431-T-G

15370370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, undefined
orthologous variants: 3120259-G-A

15370469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3120180-C-G

15370478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3120171-C-G

15370478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3120171-C-T

15370511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3120137-C-T

http://identifiers.org/hco/10/GRCh38#15370621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#3120000-C-A

15370770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, undefined
orthologous variants: 3119866-T-C

15370782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, undefined
orthologous variants: 3119854-G-A

15370843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3119799-G-A

15370843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3119799-G-T

http://identifiers.org/hco/10/GRCh38#15370884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3119755-C-A

15370884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3119755-C-T

http://identifiers.org/hco/10/GRCh38#15370938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3119705-C-A

15370938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3119705-C-T

http://identifiers.org/hco/10/GRCh38#15371073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3119567-C-A

15371073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 3119567-C-G

15371073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 3119567-C-T

http://identifiers.org/hco/10/GRCh38#15371089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#3119551-A-C

15371089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 3119551-A-G

http://identifiers.org/hco/10/GRCh38#15371137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#3119519-C-A

15371210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 3119445-T-A

15371210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 3119445-T-C

15371210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 3119445-T-G

15371224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 3119429-C-G

http://identifiers.org/hco/10/GRCh38#15371419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#3119285-A-C

15372117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3118654-C-T

15372342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23522
most severe consequence: intron variant
orthologous variants: 3118375-A-G